| Used T4 bacteriophages in radioactive phosphorus to track DNA and radioactive sulfur to track proteins to determine what is the transformational material in genes. Radioactive phosphorus found in host bacteria, but no sulfur, proving once and for all DNA was the genetic material.…
For the completion of this experiment the procedures were guided with the Rainbow Transformation1 lab manual. An Escherichia coli bacterial reference plate was used to obtain colonies which were resuspended into a CaCl2 solution that was previously kept on an ice bath. The rainbow transformation mixture containing the plasmid DNA was then added to half of the E. coli cells. These cells were later placed into a water bath set to 42ºC and “heat shocked” to promote the entrance of DNA into the cells. Moreover, a Recovery Broth was added to the sample and the sample was left undisturbed for 30 minutes at room temperature so the “heat shocked” bacteria would acquire the antibiotic resistance gene.…
Genetic transformation is one of the most important processes in biotechnology. Essentially, genetic transformation involves the process where a cell (in this lab, a bacterial cell) takes up foreign DNA from its surroundings and incorporates it into its own DNA. This gene transfer is accomplished with the aid of a plasmid, a…
7) In gene cloning, the bacterial cells take up the recombinant plasmid DNA through a process called transformation. Bacterial cells can be transformed using electric pulsation or heat. The short electric pulse or a brief rise in temperature causes openings in the plasma membrane. The bacterial cells make copies of the recombinant plasmid DNA during cell…
When a bacterium integrates a piece of DNA into its genome, bacterial transformation has occurred. In this experiment bacterial transformation will be done using calcium chloride/heat shock. This is done by incorporating the plasmids into chemically competent cells that were made permeable by the calcium chloride solution and heat shock. In 1928, Frederick Griffith, a physician from London, was he first person to experiment with bacterial transformation. He permanently transformed a safe, nonpathogenic bacterial strain of pneumococcus into a deadly pathogenic strain. [1]…
"In Griffith's 1928 experiment demonstrating bacterial transformation, injection of live S bacteria resulted in ________ mice, injection of live R bacteria resulted in ________ mice, and simultaneous injection of heat-killed S cell components and live R bacteria resulted in ________ mice:"…
The pGLO lab is a lab where students attempt to put the genes that make a jelly fish glow into E. Coli. After a process called transformation, the process in which a cell takes up and expresses a new piece of genetic information, the E. Coli will be able to glow and will be antibiotic resistant. The students first need to learn a couple of techniques before they are able to begin this lab. The first technique they will need is how to keep their environment sterile. They must learn to only open their tools, and other supplies for as long as they need, and keep them from touching anything. They must also learn that tools can never be shared between specimens, and when they use a tool, they should dispose of it and get a new one. Next they need to learn how to transfer a bacterial colony. To do this, one must use a sterile loop and scrape one colony off of the dish. Then they must insert the loop into…
Transformation is one of three processes for horizontal gene transfer by which genetic material passes from bacterium to another. “It is the acting of altering a genetic cell resulting from putting together exogenous genetic material from its surroundings through the cell membrane(s),”(Wikipedia, 2017, p.1).…
1. The process by which one strain of bacteria is apparently changed into another strain is called.…
In the first part of this lab, E.coli cells were transformed with an R-plasmid carrying a tetracycline resistant gene, giving rise to tetracycline resistant E.coli strain. This was accomplished through transformation, which allowed E.coli to directly uptake the naked DNA molecule carrying the antibiotic resistant gene (1). However, in order to take up the DNA and incorporate them into their genome via recombination, cells must be competent (1). Therefore, E.coli cells which are not competent under normal conditions were treated with cold and high concentration of CaCl2, in order to make them artificially competent (1). The transformants were grown on the LB with the tetracycline antibiotic, and on the LB without the tetracycline. Then the viable competent cells and the viable cells were counted to calculate the frequency of transformation.…
Griffith had two strains of bacterium, one pathogenic (III-S) and one non pathogenic (II-R). The mice injected with pathogenic died and the mice injected with the non pathogenic cells were alive and healthy. Pathogenic cells that were heated treated were injected into the mice and did not cause harm. However, when the heat treated pathogenic cells were mixed with non pathogenic cells caused some of the living cells to become pathogenic. The new trait of pathogenicity was inherited by all the descendants of the transformed bacteria.…
Lastly, he injected non-virulent pneumonia and virulent pneumonia that had been heated and killed, into a mouse. This time the mouse died. Griffith speculated that the killed virulent bacteria had passed on a characteristic to the non-virulent one to make it virulent. He believed this characteristic was in the inheritance molecule. This passing on of the inheritance molecule was what he called transformation.…
They then conducted a test on each of the component available in the lysate to identify the transforming factor. They first incubated the heat-killed S lysate with an enzyme, known as SIII, in which it consumed the polysaccharide coat surrounding the bacteria. Next, they tested for the transforming factor on the polysaccharide coatless S lysate. They found that the polysaccharide coatless S lysate was still able to transform producing bacteria. The R strain was producing a new S polysaccharide coat from the…
References: Arnold, J., 1898. Ueber Structur und Architectur der Zellen: I. Mitteilung. Arch. Mikrosk. Anat. Entwickl.Gesch. 52, 134 – 151. Avery, O.T., MacLeod, C.M., McCarty, M., 1944. Studies of the chemical nature of the substance inducing transformation of pneumococcal types. Induction of transformation by a deoxyribonucleic acid fraction isolated from pneumococcus type III. J. Exp. Med. 79, 137 – 158. Boveri, T., 1888. Zellenstudien II: Die Befruchtung und Teilung des Eies von Ascaris megalocephala. Jena. Zeit. Naturwiss. 22, 685 – 882.…
(ii) It forms a small amount of chloride ion in water, so gives a positive result for the chloride test.…